Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate

CAS : 184177-81-9

Ref. 3D-FP155949

Informations sur le produit

• Nom: Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate
• Synonymes: Carbamic acid, [4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-, phenyl ester, Phenyl 4-(4-(4-Hydroxyphenyl)Piperazin-1-Yl)Phenylcarbamate, Phenyl N-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]carbamate, [4-[4-(4-Hydroxy-phenyl)-piperazin-1-yl]-phenyl]-carbamic acid phenyl ester, carbamic acid, N-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-, phenyl ester, {4-[4-(4-Hydroxyphenyl)-1-Piperazinyl]-phenyl}-Carbamic acid phenyl ester

Description

Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate is a piperazine derivative. It has been shown to have an inhibitory effect on bacterial growth and is active against Gram-positive bacteria. Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate is a carbamic acid that binds to the 50S ribosomal subunit of bacteria, preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. Phenyl (4-(4-(4-hyd

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 389.45 g/mol
• Formule: C₂₃H₂₃N₃O₃
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C23H23N3O3/c27-21-12-10-20(11-13-21)26-16-14-25(15-17-26)19-8-6-18(7-9-19)24-23(28)29-22-4-2-1-3-5-22/h1-13,27H,14-17H2,(H,24,28)
• Code InChI: InChIKey=IKRKMYDCUZYKHX-UHFFFAOYSA-N
• SMILES: O=C(Nc1ccc(N2CCN(c3ccc(O)cc3)CC2)cc1)Oc1ccccc1